[0001] The present invention is concerned with reducing the interdiffusion when subjected
to elevated temperatures of a metallic-type electrical conductor or semiconductor
and a second and different metallic-type electrical conductor or semiconductor which
are in intimate contact with each other. The process of the present invention is suitable
for various processing steps in preparing an article which involve elevated temperatures
and is also suitable for preventing interdiffusion during the operation of an article
at elevated temperatures.
[0002] The process of the present invention is especially advantageous for use during the
fabrication of metallic contacts to metallic-type conductors and/or semiconductors,
and particularly when shallow junctions or interfaces are involved. The present invention
is particularly concerned with employing certain controlled gaseous atmospheres during
the time the article being treated is subject to elevated temperatures.
[0003] Typical semiconductor devices are multilayer structures which include a substrate
of a semiconductor upon which is provided an intermediate layer of a conductor or
semiconductor on top of which is provided another conductor or semiconductor layer
of a material different from that of the intermediate layer. In addition, electrical
contacts are normally provided on at least the top surface of the upper layer. Also,
electrical contact might be provided on the underside of the semiconductor substrate.
These electrical contacts are usually provided by subjecting the multilayer structure
and material for the contacts to .elevated temperatures to cause fusion of the materials.
[0004] This type of procedure, however, is conducive to interdiffusion or migration at the
interface of the material of the intermediate layers and the material of the top layer.
This interdiffusion, in turn, can result in material from the intermediate layer contaminating
the top surface of the upper layer thereby significantly altering the electrical characteristics
of the article. This can also result in the material from the top layer migrating
all the way to the underside of the semiconductor substrate, thereby causing short
circuiting.
[0005] In order to minimize oxidation as well as interdiffusion, the heating is normally
carried out in an inert atmosphere. However, the problem of interdiffusion still persists
and is especially detrimental when preparing devices having shallow junctions or interfaces.
[0006] In addition, when various semiconductor devices are operated, depending upon their
particular intended use, they may be subjected to very high temperatures. Thus, the
operation, when at elevated temperature and depending upon the environment, can eventually
result in failure of the device due to interdiffusion of adjacent conductive and/or
semiconductive layers.
[0007] The present invention as claimed is concerned with reducing the interdiffusion when
subjected to elevated temperatures of a first metallic-type electrical conductor or
semiconductor and a second and different metallic--type electrical conductor or semiconductor
which is adjacent to and in intimate contact with the first metallic-type electrical
conductor and/or semiconductor. The first metallic-type electrical conductor and/or
semiconductor and the second and different metallic-type electrical conductor and/or
semiconductor have different electronegativities. The electronegativity of a material
is the measure of the ability of the material to attract electrons. The greater the
ability, the higher the electronegativity of the material.
[0008] The term "metallic-type" as used herein refers to electrically conductive metals,
electrically conductive mixtures of metals, electrically conductive metal alloys,
as well as nonmetallic materials, such as highly doped polycrystalline silicon or
intermetallic silicides which, nevertheless, have electrical conductivities of the
magnitude generally possessed by metals.
[0009] The process of the present invention comprises subjecting or exposing at least one
surface of at least one of the metallic-type electrical conductors or semiconductors
when at elevated temperature to a gas. The gas contains at least one type of molecule
which changes the surface potential of the exposed metallic-type conductor and/or
semiconductor by increasing its work function when it is more electronegative than
the other metallic-type conductor or semiconductor or by decreasing its work function
when it is less electronegative than the other metallic-type conductor or semiconductor,
thereby reducing the interdiffusion of the conductors and/or semiconductors.
[0010] The work function is the threshold energy needed to release the electron from the
surface. Work function can be measured by the energy of light needed to cause release
of an electron from the surface of a particular material or according to procedures
specified in B. Gysae and S. Wagener: Z. Physik 115,296 (1940); and J.C.P. Mignolet:
Discussions Faraday Society 8, 326 (1950).
[0011] Figs. 1 and 2 are graphs illustrating the backscattering results obtained by subjecting
Au-Cr-Al
20
3 structures to'elevated temperatures in different atmospheres.
[0012] The structures which are subjected to the process of the present invention include
at least two layers adjacent to and in intimate contact with each other. One of the
layers contains a first metallic-type electrical conductive material and/or semiconductor,
while the other layer contains a second and different metallic-type electrical conductive
material and/or semiconductor. The electronegativity of the first conductor and/or
semiconductor is different from that of the second conductor and/or semiconductor.
[0013] The metallic-type material can be an electrically conductive metal, mixture of electrically
conductive metals, electrically conductive metallic alloy, as well as nonmetallic
material, such as highly doped polysilicon or intermetallic silicides which, nevertheless,
have electrical conductivities of the magnitude generally possessed by metals. In
addition, the metallic-type layer can contain nonconducting materials as long as these
do not destroy the conductivity characteristics of the layer to an undesired extent.
[0014] Examples of some metallic-type materials advantageously processed according to the
present invention include gold, chromium, cobalt, copper, palladium, platinum, and
aluminum. The present invention also contemplates treatment of layers containing semiconductive
materials, such as silicon, polycrystalline silicon, and GaAs. Moreover, the layers
treated can contain mixtures of metallic-type materials and semiconductors.
[0015] The preferred structures treated according to the present invention include at least
two layers which are adjacent each other and in intimate contact with each other wherein
one of the layers is present on top of the other layers. Most preferably the top layer
is of a metallic-type material. Particular structures which are especially benefited
by the present invention include those which contain an upper layer of a metal which
is very resistant to oxidation, especially at elevated temperatures, such as gold,
which is positioned on top of a layer of a different metallic-type material, such
as chromium, cobalt or copper, or of a semiconductor, such as silicon, polycrystalline
silicon, or GaAs. When desired, the layers can contain mixtures or alloys of these
metals. The process is most advantageous when the structures are of relatively thin
layers, such as about 10 to about 500 nm thick, and preferably about 50 to about 300
nm thick.
[0016] Semiconductor devices employing an upper layer of gold, an intermediate layer of
one or more of the other metals or semiconductors mentioned hereinabove, and a substrate
of a semiconductor, such as gallium arsenide are examples of devices which can be
treated according to the present invention. When fabricating such types of semiconductor
devices, metallic electrical contacts are provided on the top surface of the gold
at preselected locations and sometimes at the underside of the semiconductor substrate
whereby an electrical connection between the two can be provided by means of wire.
This processing requires the use of elevated temperatures, such as at least about
100 C, and generally up to about 500C. Most of the structures are prepared at temperatures
of about 200 to about 350°C.
[0017] However, as discussed hereinabove, when such structures are subjected to these elevated
temperatures, interdiffusion at the interface between the gold, and the underlying
layer, such as chromium, tends to occur. With respect to a structure which includes
gold as the top surface and chromium as the intermediate or underlying layer, once
interdiffusion takes place, the chromium tends to quickly migrate to the top surface
of the gold, thereby causing problems with respect to reliability of the device.
[0018] For instance, since chromium is much more susceptible to oxidation than is gold,
this migration could eventually result in formation of areas of chrome oxide on the
top surface which would act as an insulator and hinder electrical contact with the
top surface.
[0019] Migration through the, gold is accelerated, since the gold layer as normally deposited
by vapor deposition is polycrystalline, thereby providing pathways for the chromium
or other material to migrate. Accordingly, the present invention is preferably concerned
with treating those structures wherein the top surface is of a polycrystalline-type
material. The gold inherently forms a polycrystalline structure when prepared according
to vacuum deposition in the film thicknesses experienced according to the present
invention.
[0020] In addition, the interdiffusion can further cause the gold to migrate through the
intermediate layer and through the semiconductive substrate, thereby causing short
circuiting.
[0021] In order to minimize and, preferably, substantially eliminate this interdiffusion
at the interface, it has been discovered, according to the present invention, that
when the structure is subjected to elevated temperatures (e.g. about 100°C and above),
at least one surface of at least one of the metallic-type electrical conductors or
semiconductors, and preferably at least the top surface of the upper layer, is to
be exposed to a gas, wherein the gas contains at least one type of molecule which
changes the surface potential of the layer exposed to the gas by increasing its work
function when it is more electronegative than the layer adjacent it, or which decreases
its work function when it is less electronegative than the layer adjacent it.
[0022] When the gas is a mixture of gases, the relative amount of the component gas in the
mixture which changes the surface potential in the manner desired is to be sufficient
so that the effect of the mixture of gases is such as to change the surface potential
in the desired manner or direction (i.e., decrease or increase the work function as
required).
[0023] The determination of whether a particular gas or mixture of gases increases or decreases
the work function of a particular surface can be readily determined by persons skilled
in the art by the techniques referred to hereinabove. In addition, many gases have
already been tested and reported as to the manner in which they alter the work function
of particular materials. Along these lines, see Somorjai, G.A. - Principles of Surface
Chemistry, Prentice-Hall, Inc., Englewood Cliffs, New Jersey (1972), pages 249, 158
and 159.
[0024] The preferred structures treated according to the present invention are preferably
treated by positioning the structure in a chamber with the substrate resting on a
support and the top surface of the upper layer facing upwards with the gas being supplied
through the chamber. The gas upon contact with the upper surface of a polycrystalline
layer, such as gold, will diffuse rapidly down to the interface, since the grain boundaries
of the polycrystalline structure tend to act as pathways.
[0025] Normally, the structures are subjected to elevated temperatures at any one time from
a few minutes to about two hours, and more usually from about 10 minutes to about
one hour under normal processing and/or operating conditions.
[0026] It has been found, according to the present invention, with structures wherein the
upper layer is gold and the intermediate layer is a material less electronegative
than gold, such as chromium, silicon, cobalt, and copper, that both carbon monoxide
and hydrogen increase the work function of the gold layer and are suitable for carrying
out the present invention. The carbon monoxide is much more effective than the hydrogen.
In addition, it is noted that steam, air, and oxygen actually reduce the work function
of the surface of the gold and, therefore, result in an increase in the interdiffusion
of the gold and the material adjacent thereto.
[0027] It is desirable to use mixtures of carbon monoxide and another gas, such as air,
so long as sufficient carbon monoxide is present in the mixture to effect the desired
minimization of the interdiffusion. For instance, it was noted that a ratio of 1:1
air and carbon monoxide actually prevented the interdiffusion of gold and chromium.
[0028] In addition, it has been found, according to the present invention, that structures
of platinum on top of a layer of material which is less electronegative than the platinum,
such as chromium, can be processed according to the present invention employing oxygen
or air. Oxygen and air actually increase the work function of platinum as opposed
to their effect on the work function of gold.
[0029] In order to further illustrate the present invention; the following examples are
presented.
Example I
[0030] A structure having a substrate of A1
20
3 upon which is provided a layer of about 200 to about 300 nm chromium and a vapor
deposited layer of about 200 to about 300 nm of gold on the chromium is provided.
The structure (the gold facing upward) is subjected to temperatures of about 250
0C for one hour in a mixture of about 1:1 volume ratio of air and carbon monoxide.
After this, the structure is tested for interdiffusion by using He+
- ion backscattering spectrometry. This procedure involves counting the number of He
+ ions reflected back from the sample using He
+ at 2,8 MeV, and the counts times 10
-3 are plotted against the channel number and reproduced in Fig. 1. Also plotted in
Fig. 1 is the backscattering data achieved from the same structure which has not been
subjected to the elevated temperatures. As seen from Fig. 1, the 1:1 ratio of air
and carbon monoxide resulted in completely stopping the interdiffusion.
Example II
[0031] Example I is repeated except that the structure is heated in air for one hour at
250°C. The results obtained are presented in Fig. 2, and as apparent from Fig. 2,
a comparison of that treatment with the reference shows a significant interdiffusion
of the gold and chromium. Note the yield between the 300 and 400 channel numbers.
As noted, for the reference within that range, the yield is about 0. On the other
hand, significant yields are obtained when the heating is carried out in air.
Example III
[0032] Example I is repeated except that the structure is heated in a mixture of about 5
parts by volume of air per 1 part by volume carbon monoxide at 250
0C for about one hour. The results obtained are shown in Fig. 2. As apparent from Fig.
2, the air and carbon monoxide mixture of 5:1 resulted in some reduction of the interdiffusion
of the gold and chromium, but not the complete elimination of such as achieved by
a ratio of 1:1 of air and carbon monoxide.
1. A method for reducing the interdiffusion when at elevated temperature of a first
metallic-type electrical conductive material or a first semiconductive material or
mixtures thereof, and a second and different metallic-type electrical conductive material
or second and different semiconductive material or mixtures thereof which is adjacent
to and in intimate contact with the-first material; wherein the electronegativity
of the first material-is different from the electronegativity of the second material,
which comprises when at elevated temperature of at least about 100°C exposing at least
one surface of at least one of said first material and said second material to a gas
containing at least one type of molecule which changes the surface potential of the
material exposed by increasing its work function when it is more electronegative than
the other material or by decreasing its work function when it is less electronegative
than the other material, and wherein said gas contains CO or O2 or both; and thereby reducing the interdiffusion of the first and second materials
at their interface and at elevated temperature.
2. The method of claim 1 wherein the first material is located on top of the second
material.
3. The method of a previous claim wherein said first material is a layer comprising
a metallic-type electrical conductive material.
4. The method of any previous claim wherein the first and second materials are layers
about 10 to about 500 nm thick.
5. The method of any previous claim wherein the first and second materials are layers
about 50 to about 300 nm thick.
6. The method of claim 3 wherein said metallic-type electrical conductive material
is polycrystalline gold.
7. The.method of any previous claim wherein said second material is a layer of a material
selected from the group of chromium, cobalt, copper, silicon, and mixtures thereof.
8. The method of claim 2 or 7, wherein the second material is located on top of a
semiconductive substrate.
9. The method of claim 8 wherein said substrate is gallium arsenide.
10. The method of any previous claim wherein said elevated temperature is up to about
500°C.
11. The method of any previous claim wherein said elevated temperature is about 200
to about 350°C.
12. The method of any previous claim wherein said gas is a mixture of carbon monoxide
and air.
13. The method of claim 12 wherein said gas is a mixture of carbon monoxide and air
in a ratio of about 1:1.
14. The method of claim 6 wherein said second material is less electronegative than
said gold.
15. The method of claim 3 wherein said metallic-type electrical conductive material
is platinum.
16. The method of claim 15,wherein said second material is less electronegative than
said platinum.
17. The method of claim 16 wherein the gas contains 02.